A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13939557



Internal ID3941373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112587036..112621108hg38UCSC Ensembl
chr10:114346795..114380867hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3834073
hg1934073
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624585
Supporting Variants
SamplesHG03193
Known GenesVTI1A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13939557
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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